Canonical Allele Identifier: CA890972305

Gene: SDHB

Linked Data

• dbSNP Id: rs1234224040
• MyVariant Identifiers: chr1:g.17354642_17354646del (hg19) ; chr1:g.17028147_17028151del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028147_17028151del , CM000663.2:g.17028147_17028151del	GRCh38
NC_000001.10:g.17354642_17354646del , CM000663.1:g.17354642_17354646del	GRCh37
NC_000001.9:g.17227229_17227233del	NCBI36
NG_012340.1:g.31020_31024del , LRG_316:g.31020_31024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-286_253-282del	ENSP00000481376.2:n.253-286_253-282del
ENST00000491274.6:c.382-286_382-282del	ENSP00000480482.2:n.382-286_382-282del
ENST00000375499.8:c.424-286_424-282del MANE Select	ENSP00000364649.3:n.424-286_424-282del
ENST00000375499.7:c.424-286_424-282del	ENSP00000364649.3:n.424-286_424-282del
ENST00000463045.2:c.253-286_253-282del	ENSP00000481376.1:n.253-286_253-282del
ENST00000475506.1:n.341-286_341-282del
ENST00000485515.5:n.358-286_358-282del
ENST00000491274.5:c.382-286_382-282del	ENSP00000480482.1:n.382-286_382-282del
NM_003000.2:c.424-286_424-282del , LRG_316t1:c.424-286_424-282del	NP_002991.2:n.424-286_424-282del
NM_003000.3:c.424-286_424-282del MANE Select	NP_002991.2:n.424-286_424-282del